• Clarissa M Koch, Andrew D Prigge, Kishore R Anekalla, Avani Shukla, Hanh Chi Do Umehara, Leah Setar, Jairo Chavez, Hiam Abdala-Valencia, Yuliya Politanska, Nikolay S Markov, Grant R Hahn, Taylor Heald-Sargent, L Nelson Sanchez-Pinto, William J Muller, Benjamin D Singer, Alexander V Misharin, Karen M Ridge, and Bria M Coates.
• Northwestern University, Medicine , Chicago, Illinois, United States.
• Am. J. Respir. Cell Mol. Biol. 2021 Nov 3.

AbstractSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has infected more than 180 million people since the onset of the global pandemic. Despite similar viral load and infectivity rates between children and adults, children rarely develop severe illness. Differences in the host response to the virus at the primary infection site are among the mechanisms proposed to account for this disparity. Our objective was to investigate the host response to SARS-CoV-2 in the nasal mucosa in children and adults and compare it to the host response to respiratory syncytial virus (RSV) and influenza virus (IV). We analyzed clinical outcomes and gene expression in the nasal mucosa of 36 children with SARS-CoV-2, 24 children with RSV, 9 children with IV, 16 adults with SARS-CoV-2, and 7 healthy pediatric and 13 healthy adult controls. In both children and adults, infection with SARS-CoV-2 led to an interferon response in the nasal mucosa. The magnitude of the interferon response correlated with the abundance of viral reads, not the severity of illness, and was comparable between children and adults infected with SARS-CoV-2 and children with severe RSV infection. Expression of ACE2 and TMPRSS2 did not correlate with age or presence of viral infection. SARS-CoV-2-infected adults had increased expression of genes involved in neutrophil activation and T cell receptor signaling pathways compared to SARS-CoV-2-infected children, despite similar severity of illness and viral reads. Age-related differences in the immune response to SARS-CoV-2 may place adults at increased risk of developing severe illness. This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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